A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184863



Internal ID20751903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32708754..32719802hg38UCSC Ensembl
chr10:32997682..33008730hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811049
hg1911049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443051
Supporting Variants
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184863
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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